Department of Medical Chemistry, Kansai Medical University, Moriguchi 570-8506, Japan,; Department of Biomedical Engineering, Osaka Institute of Technology, Osaka 535-8585, Japan,.
Department of Anesthesiology, Osaka Medical College, Takatsuki 569-8686, Japan.
J Biol Chem. 2012 Mar 23;287(13):10403-10413. doi: 10.1074/jbc.M111.271866. Epub 2012 Feb 6.
4-Nitrophenylphosphatase domain and non-neuronal SNAP25-like protein homolog 1 (NIPSNAP1) is a molecule of physiologically unknown function, although it is predominantly expressed in the brain, spinal cord, liver, and kidney. We identified NIPSNAP1 as a protein that interacts with the neuropeptide nocistatin (NST) from synaptosomal membranes of mouse spinal cord using high-performance affinity latex beads. NST, which is produced from the same precursor protein as an opioid-like neuropeptide nociceptin/orphanin FQ (N/OFQ), has opposite effects on pain transmission evoked by N/OFQ. The calculated full-length pre-protein of NIPSNAP1 was 33 kDa, whereas the N-terminal truncated form of NIPSNAP1 (29 kDa) was ubiquitously expressed in the neuronal tissues, especially in synaptic membrane and mitochondria of brain. The 29-kDa NIPSNAP1 was distributed on the cell surface, and NST interacted with the 29-kDa but not the 33-kDa NIPSNAP1. Although intrathecal injection of N/OFQ induced tactile allodynia in both wild-type and NIPSNAP1-deficient mice, the inhibition of N/OFQ-evoked tactile allodynia by NST seen in wild-type mice was completely lacking in the deficient mice. These results suggest that NIPSNAP1 is an interacting molecule of NST and plays a crucial role in pain transmission.
4-硝基苯磷酸酶结构域和非神经元 SNAP25 样蛋白同源物 1(NIPSNAP1)是一种生理功能未知的分子,尽管它主要在大脑、脊髓、肝脏和肾脏中表达。我们使用高性能亲和乳胶珠从鼠脊髓突触体膜中鉴定出 NIPSNAP1 是一种与神经肽 nocistatin(NST)相互作用的蛋白。NST 与阿片样神经肽 nociceptin/orphanin FQ(N/OFQ)来自同一前体蛋白,对 N/OFQ 诱发的疼痛传递具有相反的作用。NIPSNAP1 的全长前蛋白计算为 33 kDa,而 NIPSNAP1 的 N 端截断形式(29 kDa)在神经元组织中普遍表达,特别是在大脑的突触膜和线粒体中。29 kDa 的 NIPSNAP1 分布在细胞表面,NST 与 29 kDa 的 NIPSNAP1 相互作用,但与 33 kDa 的 NIPSNAP1 不相互作用。尽管鞘内注射 N/OFQ 在野生型和 NIPSNAP1 缺陷型小鼠中均诱导触觉过敏,但在野生型小鼠中观察到的 NST 抑制 N/OFQ 诱发的触觉过敏在缺陷型小鼠中完全缺失。这些结果表明 NIPSNAP1 是 NST 的相互作用分子,在疼痛传递中发挥关键作用。